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. 2014 Jul;144(1):115–124. doi: 10.1085/jgp.201411179

Figure 1.

Figure 1.

Measuring bi-ionic potential of the TMEM16A current. (A) Activation of Cl current (top) in an excised inside-out patch expressing TMEM16A in symmetrical 140 mM [Cl]. (Bottom) The digital signal used to switch between the solutions containing zero-Ca2+ and 20 µM of free [Ca2+]. (B) Current-clamp (I = 0) recordings to monitor the change of bi-ionic potentials upon the switch of anion solutions on the intracellular side. Intracellular solutions contained 20 µM of free [Ca2+] throughout the recording. Same patch as in A. (Bottom) The digital signal for triggering solution exchange. (C) Bi-ionic potentials measured by voltage-clamp recordings. The two panels were recordings from two different patches consisting of currents of different amplitudes (see the scale of the y axis). Different values of Erev were obtained as exemplified in the bi-ionic condition of SCN/Cl. (D) The SCN/Cl bi-ionic potential as a function of the current amplitude at 40 mV in symmetrical 140 mM Cl. Each data point was from an independent patch measured either by the voltage-clamp or by the current-clamp recording.